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Open AccessJournal ArticleDOI

[6n]methyl adenine in the nuclear dna of a eucaryote, tetrahymena pyriformis

TLDR
DNA isolated from macronuclei of the ciliate, Tetrahymena pyriformis, has been found to contain [6N]methyl adenine (MeAde); this represents the first clear demonstration of significant amounts of MeAde in the DNA of a eucaryote.
Abstract
DNA isolated from macronuclei of the ciliate, Tetrahymena pyriformis, has been found to contain [6N]methyl adenine (MeAde); this represents the first clear demonstration of significant amounts of MeAde in the DNA of a eucaryote. The amounts of macronuclear MeAde differed slightly between different strains of Tetrahymena, with approximately 0.65–0.80% of the adenine bases being methylated. The MeAde content of macronuclear DNA did not seem to vary in different physiological states. The level of MeAde in DNA isolated from micronuclei, on the other hand, was quite low (at least tenfold lower than in macronuclear DNA).

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Journal ArticleDOI

DNA modification mechanisms and gene activity during development.

TL;DR: This article suggests mechanisms that may account for the differentiated state of dividing or nondividing cells and that also attempt to explain the ordered switching on or off of genes during development.
Book ChapterDOI

Isolation of micro- and macronuclei of Tetrahymena pyriformis.

TL;DR: This chapter discusses the isolation of micro- and macronuclei of Tetrahymena Pyriformis and suggests that these two nuclei may be used as a model system to explore the mechanisms whereby the same genetic information is maintained in different structural and functional states in eukaryotic cells.
Journal ArticleDOI

N6-methyladenine: the other methylated base of DNA

TL;DR: Interestingly, even if adenine methylation is usually considered a bacterial DNA feature, the presence of m6A has been found in protist and plant DNAs, highlighting the importance of considering m 6A as the sixth element of DNA.
Journal ArticleDOI

DNA N 6 -methyladenine: a new epigenetic mark in eukaryotes?

TL;DR: Recent publications documenting the presence of 6mA in Chlamydomonas reinhardtii, Drosophila melanogaster and Caenorhabditis elegans are discussed and possible roles for this DNA modification in regulating transcription, the activity of transposable elements and transgenerational epigenetic inheritance are considered.
Journal ArticleDOI

Comparison of the sequences of macro- and micronuclear DNA of Tetrahymena pyriformis

TL;DR: Findings place severe constraint on possible models concerning the structure of the Tetrahymena macronucleus, and are very different from the situation observed in Stylonychia where it has been suggested that only a small percentage of the sequences in micronuclei are present in significant amounts in macron nuclei.
References
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Journal ArticleDOI

Methylation of DNA in developing sea urchin embryos.

TL;DR: The data suggest that DNA 5-methylcytosine is synthesized at the polymer level in developing sea urchin embryos as it is known to occur in other organisms.
Journal ArticleDOI

Mouse nuclear satellite dna, 5-methylcytosine content, pyrimidine isoplith distribution and electron microscopic appearance.

TL;DR: Nuclear satellite DNA of high specific activity labelled with [ 3 H- methyl ]- l -methionine and 32 P was isolated from newborn mice and from cultured mouse embryo cells and found to have more than twice the molar concentration of 5-methylcytosine than the main band of nuclear DNA.
Journal ArticleDOI

The in vivo methylation of DNA in mouse fibroblasts.

TL;DR: Experiments with synchronised cell cultures demonstrated that cytosine methylation occurred within an hour of the synthesis of DNA in the S phase of the cell cycle, and showed that the 5-methylcytosine of DNA so formed is stable, no evidence being found for its demethylation, deamination or excision from the polymer.
Journal ArticleDOI

Regulierung der DNS-Menge im Makronucleus von Tetrahymena

TL;DR: The amount of Feulgen-positive material in the macronucleus of Tetrahymena pyriformis HSM was determined by means of microphotometry in different stages of the cell cycle and in cell lines to maintain the mean DNA amount and the degree of variation.
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